SELECTED PUBLICATIONS

Comorbidities of epilepsy: results from the Epilepsy Comorbidities and Health (EPIC) survey. Ottman R, Lipton RB, Ettinger AB, Cramer JA, Reed ML, Morrison A, Wan GJ. Epilepsia 2011;52:308-315.

Accuracy of family history information on epilepsy and other seizure disorders. Ottman R, Barker-Cummings C, Leibson CL, Vasoli VM, Hauser WA, Buchhalter JR. Neurology 2011;76:390-396.

Genetic testing in the epilepsies--report of the ILAE Genetics Commission. Ottman R, Hirose S, Jain S, Lerche H, Lopes-Cendes I, Noebels JL, Serratosa J, et al. Epilepsia 2010;51:655-670.

Validation of a brief screening instrument for the ascertainment of epilepsy. Ottman R, Barker-Cummings C, Leibson CL, Vasoli VM, Hauser WA, Buchhalter JR. Epilepsia 2010;51:191-197.

Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+. Poduri A, Wang Y, Gordon D, Barral-Rodriguez S, Barker-Cummings C, Ulgen A, Chitsazzadeh V, et al. Neurology 2009;73:1264-1272.

Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Rosanoff MJ, Ottman R. Neurology 2008;71:567-571.

Phenotypic concordance in 70 families with IGE-implications for genetic studies of epilepsy. Kinirons P, Rabinowitz D, Gravel M, Long J, Winawer M, Senechal G, Ottman R, et al. Epilepsy Research 2008;82:21-28.

Ethical, legal, and social dimensions of epilepsy genetics. Shostak S, Ottman R. Epilepsia 2006;47:1595-1602.

Classification of partial seizure symptoms in genetic studies of the epilepsies. Choi H, Winawer MR, Kalachikov S, Pedley TA, Hauser WA, Ottman R. Neurology 2006;66:1648-1653.

Familial clustering of seizure types within the idiopathic generalized epilepsies. Winawer MR, Marini C, Grinton BE, Rabinowitz D, Berkovic SF, Scheffer IE, Ottman R. Neurology 2005;65:523-528.

Recruitment of families for genetic studies of epilepsy. Ottman R, Berenson K, Barker-Cummings C. Epilepsia 2005;46:290-297.

Analysis of genetically complex epilepsies. Ottman R. Epilepsia 2005;46 Suppl 10:7-14.

LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Ottman R, Winawer MR, Kalachikov S, Barker-Cummings C, Gilliam TC, Pedley TA, Hauser WA. Neurology 2004;62:1120-1126.

Genetic influences on myoclonic and absence seizures. Winawer MR, Rabinowitz D, Pedley TA, Hauser WA, Ottman R. Neurology 2003;61:1576-1581.

Evidence for distinct genetic influences on generalized and localization-related epilepsy. Winawer MR, Rabinowitz D, Barker-Cummings C, Scheuer ML, Pedley TA, Hauser WA, Ottman R. Epilepsia 2003;44:1176-1182.

Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24. Winawer MR, Martinelli Boneschi F, Barker-Cummings C, Lee JH, Liu J, Mekios C, Gilliam TC, et al. Epilepsia 2002;43:60-67.

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Kalachikov S, Evgrafov O, Ross B, Winawer M, Barker-Cummings C, Martinelli Boneschi F, Choi C, et al. Nature Genetics 2002;30:335-341.

ILAE genetics commission conference report: molecular analysis of complex genetic epilepsies. Anderson E, Berkovic S, Dulac O, Gardiner M, Jain S, Laue Friis M, Lindhout D, et al. Epilepsia 2002;43:1262-1267.

Autosomal dominant partial epilepsy with auditory features: defining the phenotype. Winawer MR, Ottman R, Hauser WA, Pedley TA. Neurology 2000;54:2173-2176.

Are generalized and localization-related epilepsies genetically distinct? Ottman R, Lee JH, Hauser WA, Risch N. Archives of Neurology 1998;55:339-344.

Genetic epidemiology of epilepsy. Ottman R. Epidemiologic Reviews 1997;19:120-128.

Is the comorbidity of epilepsy and migraine due to a shared genetic susceptibility? Ottman R, Lipton RB. Neurology 1996;47:918-924.

Clinical indicators of genetic susceptibility to epilepsy. Ottman R, Lee JH, Risch N, Hauser WA, Susser M. Epilepsia 1996;37:353-361.

Relations of genetic and environmental factors in the etiology of epilepsy. Ottman R, Annegers JF, Risch N, Hauser WA, Susser M. Annals of Neurology 1996;39:442-449.